Jonathan Berg
Impact in
- Genetics top 0.5%
- Vascular Anomalies and Treatments
-
- Tracheal and airway disorders
- Pulmonary Hypertension Research and Treatments
Papers in
- Genetics 14
- Vascular Anomalies and Treatments 12
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
-
- Tracheal and airway disorders 8
- Pulmonary Hypertension Research and Treatments 5
- Co-authors
- Douglas A. Marchuk (10 shared papers)Mary Porteous (7 shared papers)Carol J. Gallione (9 shared papers)Charles E. Jackson (5 shared papers)David W. Johnson (3 shared papers)Alan E. Guttmacher (4 shared papers)Timothy T. Stenzel (4 shared papers)Raju Kucherlapati (1 shared paper)
- Journals
- European Journal of Human Genetics (4 papers)Journal of Medical Genetics (3 papers)Human Genetics (2 papers)Frontiers in Immunology (2 papers)Human Mutation (2 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Jonathan Berg
41 papers receiving 3.0k citations
Jonathan Berg's Hit Papers
Peers
Comparison fields: 5 of 95
- Genetics 1.3k
- Pulmonary and Respiratory Medicine 1.2k
- Neurology 290
- Marketing 195
- Surgery 595
Countries citing papers authored by Jonathan Berg
This map shows the geographic impact of Jonathan Berg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jonathan Berg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan Berg more than expected).
Fields of papers citing papers by Jonathan Berg
This network shows the impact of papers produced by Jonathan Berg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jonathan Berg. The network helps show where Jonathan Berg may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan Berg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2 Hit paper breakdown → | 1996 | 908 |
| 2 | Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia Hit paper breakdown → | 2001 | 564 |
| 3 | 1997 | 202 | |
| 4 | 2014 | 141 | |
| 5 | 1995 | 138 | |
| 6 | 2009 | 129 | |
| 7 | 1996 | 97 | |
| 8 | 1995 | 91 | |
| 9 | 2014 | 80 | |
| 10 | 1998 | 80 | |
| 11 | 2004 | 67 | |
| 12 | 2004 | 56 | |
| 13 | 2003 | 55 | |
| 14 | 2017 | 45 | |
| 15 | 2001 | 42 | |
| 16 | 2007 | 35 | |
| 17 | 2000 | 33 | |
| 18 | 2009 | 31 | |
| 19 | 2018 | 28 | |
| 20 | 2007 | 28 |
About Jonathan Berg
Jonathan Berg is a scholar working on Genetics, Genetics, Pulmonary and Respiratory Medicine, Molecular Biology and Surgery, having authored 43 papers that have together received 3.1k indexed citations. Recurring topics across this work include Vascular Anomalies and Treatments (12 papers), Tracheal and airway disorders (8 papers), BRCA gene mutations in cancer (5 papers), Pulmonary Hypertension Research and Treatments (5 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and melanin and skin pigmentation (2 papers). The work is most often cited by research in Genetics (1.3k citations), Pulmonary and Respiratory Medicine (1.2k citations), Neurology (290 citations), Marketing (195 citations) and Surgery (595 citations). Jonathan Berg has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Douglas A. Marchuk, Mary Porteous, Carol J. Gallione, Charles E. Jackson, David W. Johnson, Alan E. Guttmacher, Timothy T. Stenzel, Raju Kucherlapati, Austin G. Diamond and Sang-Heon Yoon. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Human Genetics, Frontiers in Immunology and Human Mutation.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.